Canonical Allele Identifier: CA2262805582
Gene: TBX21 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.47733388_47733413delinsACGCGACCCTCTCGCGCGCGGAGGGG , CM000679.2:g.47733388_47733413delinsACGCGACCCTCTCGCGCGCGGAGGGG GRCh38
NC_000017.10:g.45810754_45810779delinsACGCGACCCTCTCGCGCGCGGAGGGG , CM000679.1:g.45810754_45810779delinsACGCGACCCTCTCGCGCGCGGAGGGG GRCh37
NC_000017.9:g.43165753_43165778delinsACGCGACCCTCTCGCGCGCGGAGGGG NCBI36
NG_012166.1:g.5145_5170delinsACGCGACCCTCTCGCGCGCGGAGGGG

Transcript Alleles

HGVS Amino-acid Change
ENST00000177694.2:c.-67_-42delinsACGCGACCCTCTCGCGCGCGGAGGGG MANE Select ENSP00000177694.1:n.-67_-42delinsACGCGACCCTCTCGCGCGCGGAGGGG
ENST00000177694.1:c.-67_-42delinsACGCGACCCTCTCGCGCGCGGAGGGG ENSP00000177694.1:n.-67_-42delinsACGCGACCCTCTCGCGCGCGGAGGGG
NM_013351.1:c.-67_-42delinsACGCGACCCTCTCGCGCGCGGAGGGG NP_037483.1:n.-67_-42delinsACGCGACCCTCTCGCGCGCGGAGGGG
XM_011524698.1:c.-67_-42delinsACGCGACCCTCTCGCGCGCGGAGGGG XP_011523000.1:n.-67_-42delinsACGCGACCCTCTCGCGCGCGGAGGGG
NM_013351.2:c.-67_-42delinsACGCGACCCTCTCGCGCGCGGAGGGG MANE Select NP_037483.1:n.-67_-42delinsACGCGACCCTCTCGCGCGCGGAGGGG